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NARROW
GeoRef Subject
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all geography including DSDP/ODP Sites and Legs
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Africa
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Limpopo Basin (1)
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North Africa
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Atlas Mountains
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Moroccan Atlas Mountains
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Maghreb (1)
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Morocco
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Southern Africa
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South Africa
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Antarctica (3)
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Asia
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Central Asia
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Far East
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Paleozoic
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sheet silicates
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Primary terms
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Africa
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Atlas Mountains
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Maghreb (1)
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Moroccan Atlas Mountains
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Middle Atlas (1)
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Rif (2)
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Southern Africa
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biochronology
Cenozoic stratigraphy of South Africa: current challenges and future possibilities
Fossil bivalves and the sclerochronological reawakening
Global biotic events evident in the Paleogene marine strata of the eastern San Francisco Bay area, California
ABSTRACT Paleogene marine strata in the eastern San Francisco Bay area are exposed in discontinuous outcrops in the various tectonic blocks. Although there are many missing intervals, the strata were previously thought to span most of the Paleocene and Eocene. Revision of biochronology and calibration to the international time scale as well as to the global oxygen isotope curve and sea-level curves indicate that the strata are latest Paleocene through middle Eocene in age and contain faunal changes that are linked to the overall global climate trends and hyperthermals of that time. The Paleocene-Eocene thermal maximum, third Eocene thermal maximum, early Eocene climatic optimum, and middle Eocene climatic optimum are all identified in the eastern San Francisco Bay marine strata. The dominance of smoothly finished, dissolution-resistant agglutinated benthic foraminiferal species corresponds with a rapid shoaling and rapid deepening (overcorrection) of the calcium compensation depth associated with the Paleocene-Eocene thermal maximum. The benthic foraminiferal extinction event was a dramatic turnover of benthic foraminiferal species that occurred shortly after the onset of the Paleocene-Eocene thermal maximum. Opportunistic species such as Bulimina , which indicate environmental stress and lower oxygen conditions, are commonly associated with the Paleocene-Eocene thermal maximum. Environmental changes similar to those observed during the Paleocene-Eocene thermal maximum also characterize the third Eocene thermal maximum, based on the agglutinated and opportunistic species. The early Eocene climatic optimum is noted by the presence of foraminiferal assemblages that indicate a stable, warmer water mass, abundant food, and an influx of terrigenous material. The onset and end of the middle Eocene climatic optimum are recognized by the dominance of siliceous microfossils. This research updates the age and environmental interpretations of the Paleogene formations occurring in the vicinity of Mount Diablo, eastern San Francisco Bay area. The revised interpretations, which are based on foraminifers and calcareous nannoplankton, make it possible to identify various global climatic and biotic events.
Radiolarian Biochronology, Detrital Zircon Geochronological and Geochemical Constraints on Provenance and Depositional Environment of Cherts in the Southern Belt of the Western Yarlung Zangbo Suture Zone, Tibet
Ammonite occurrences in North Sea cores: implications for Jurassic Arctic–Mediterranean marine seaway connectivity
Subannual stable isotope records reveal climate warming and seasonal anoxia associated with two extinction intervals across the Cretaceous-Paleogene boundary on Seymour Island, Antarctica
Biochronology, paleoenvironments, and stratigraphic sequences of the late Albian–middle Eocene fore-arc Vizcaino basin, western Baja California, Mexico
Pliocene–Pleistocene sedimentary development of the syntectonic Polis graben, NW Cyprus: evidence from facies analysis, nannofossil biochronology and strontium isotope dating
A large pterodactyloid pterosaur from the Late Cretaceous Ferron Sandstone of Utah
Abstract: Three associated incomplete wing bones of a large pterodactyloid pterosaur from the Ferron Sandstone Member of the Mancos Shale Formation of Utah are described. Based on the morphology of the bones’ articular ends, the specimen is referred to the Pteranodontoidea. Associated ammonites indicate that the specimen’s age is Middle Turonian, so it adds to the sparse worldwide record of Turonian pterosaurs. The record of pteranodontoid pterosaurs in the Western Interior Seaway of North America is reviewed, and it is suggested that pteranodontoids were not diverse.
Abstract: In 1841, Murchison coined the term Permian for strata in the Russian Urals. Recognition of the Permian outside of Russia and central Europe soon followed, but it took about a century for the Permian to be accepted globally as a distinct geological system. The work of the Subcommission on Permian Stratigraphy began in the 1970s and resulted in current recognition of nine Permian stages in three series: the Cisuralian (lower Permian) – Asselian, Sakmarian, Artinskian and Kungurian; the Guadalupian (middle Permian) – Roadian, Wordian and Capitanian; and the Lopingian (upper Permian) – Wuchiapingian and Changhsingian. The 1990s saw the rise of Permian conodont biostratigraphy, so that all Permian Global Stratigraphic Sections and Points (GSSPs) use conodont evolutionary events as the primary signal for correlation. Issues in the development of a Permian chronostratigraphic scale include those of stability and priority of nomenclature and concepts, disagreements over changing taxonomy, ammonoid v. fusulinid v. conodont biostratigraphy, differences in the perceived significance of biotic events for chronostratigraphic classification, and correlation problems between provinces. Further development of the Permian chronostratigraphic scale should focus on GSSP selection for the remaining, undefined stage bases, definition and characterization of substages, and further integration of the Permian chronostratigraphic scale with radioisotopic, magnetostratigraphic and chemostratigraphic tools for calibration and correlation.
Abstract: Establishing a Permian brachiopod biochronological scheme for global correlation is difficult because of strong provincialism during the Permian. In this paper, a brief overview of brachiopod successions in five major palaeobiogeographical realms/zones is provided. For Gondwanaland and peri-Gondwanan regions including Cimmerian blocks, Bandoproductus and Punctocyrtella (or Cyrtella ) are characteristic of the lower Cisuralian, as is Cimmeriella for the middle Cisuralian. As the Cimmerian blocks continued drifting north during the late Kungurian, accompanied by climate amelioration, contemporaneous brachiopods inhabiting these blocks showed a distinct shift from cold-water to mixed or warm-water affinities. However, coeval brachiopods in the Northern Transitional Zone (NTZ) are characterized by warm-water faunas and are associated with fusulinids in the lower Cisuralian. The Guadalupian brachiopods of the NTZ were clearly mixed between the Boreal and palaeoequatorial affinities. The end-Guadalupian is marked by the disappearance of a few characteristic genera, such as Vediproductus , Neoplicatifera and Urushtenoidea , in the Palaeotethyan region. The onset of the end-Permian mass extinction in the latest Changhsingian is clearly exhibited by the occurrence of the dwarfed and thin-shelled brachiopods commonly containing Paracrurithyris .
Abstract: Tetrapod footprints are among the most common fossil remains in continental Permian strata and thus are of biostratigraphic interest. Based on the vertical distribution of the 13 best-known Permian tetrapod ichnotaxa, three footprint biochrons are suggested for the period: (1) Dromopus – latest Carboniferous (approximately Gzhelian) to late Early Permian (approximately Artinskian), representing ichnoassemblages dominated by tracks of temnospondyls, reptiliomorphs, pelycosaurs and early diapsids; (2) Erpetopus – late Early Permian (approximately Kungurian) to late Middle Permian (approximately Capitanian), representing ichnoassemblages dominated by tracks of non-diapsid eureptiles; and (3) Paradoxichnium – Late Permian (Wuchiapingian and Changhsingian), representing ichnoassemblages dominated by tracks of medium- and large-sized parareptiles, non-diapsid eureptiles and early saurians. This is the most conservative ichnostratigraphic concept, and it may be possible to refine it to almost stage-level resolution by future comprehensive analysis, especially of Permian captorhinomorph and therapsid footprints. Other major tasks to improve Permian tetrapod footprint ichnostratigraphy include enhanced knowledge of Middle Permian tetrapod footprints, and clarification of the palaeoenvironmental factors that may control the distribution of tetrapod footprints in space and time.
Permian tetrapod biochronology, correlation and evolutionary events
Abstract: The most extensive Permian tetrapod (amphibian and reptile) fossil records from the western USA (New Mexico to Texas) and South Africa have been used to define 11 land vertebrate faunachrons (LVFs). These are, in ascending order, the Coyotean, Seymouran, Mitchellcreekian, Redtankian, Littlecrotonian, Kapteinskraalian, Gamkan, Hoedemakeran, Steilkransian, Platbergian and Lootsbergian. These faunachrons provide a biochronological framework with which to assign ages to, and correlate, Permian tetrapod fossil assemblages. Intercalated marine strata, radioisotopic ages and magnetostratigraphy were used to correlate the Permian LVFs to the standard global chronostratigraphic scale with varying degrees of precision. Such correlations identified the following significant events in Permian tetrapod evolution: a Coyotean chronofaunal event (end Coyotean); Redtankian events (Mitchellcreekian–Littlecrotonian); Olson’s gap (late Littlecrotonian); a therapsid event (Kapteinskraalian); a dinocephalian extinction event (end Gamkan); and a latest Permian extinction event (Platbergian–Lootsbergian boundary). Problems of incompleteness, endemism and taxonomy, and the relative lack of non-biochronological age control continue to hinder the refinement and correlation of a Permian timescale based on tetrapod biochronology. Nevertheless, the global Permian timescale based on tetrapod biochronology is a robust tool for both global and regional age assignment and correlation. Advances in Permian tetrapod biochronology will come from new fossil discoveries, more detailed biostratigraphy and additional alpha taxonomic studies based on sound evolutionary taxonomic principles.